首页> 美国卫生研究院文献>Plant Physiology >Focus Issue: The Agrobacterium-Plant Cell Interaction: Recognition of the Agrobacterium tumefaciens VirE2 Translocation Signal by the VirB/D4 Transport System Does Not Require VirE1
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Focus Issue: The Agrobacterium-Plant Cell Interaction: Recognition of the Agrobacterium tumefaciens VirE2 Translocation Signal by the VirB/D4 Transport System Does Not Require VirE1

机译:焦点问题:农杆菌-植物细胞相互作用:通过VirB / D4转运系统识别根癌农杆菌VirE2易位信号不需要VirE1

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摘要

Agrobacterium tumefaciens uses a type IV secretion system to deliver a nucleoprotein complex and effector proteins directly into plant cells. The single-stranded DNA-binding protein VirE2, the F-box protein VirF and VirE3 are delivered into host cells via this VirB/D4 encoded translocation system. VirE1 functions as a chaperone of VirE2 by regulating its efficient translation and preventing VirE2-VirE2 aggregation in the bacterial cell. We analyzed whether the VirE1 chaperone is also essential for transport recognition of VirE2 by the VirB/D4 encoded type IV secretion system. In addition, we assayed whether translocation of VirF and VirE3, which also forms part of the virE operon, is affected by the absence of VirE1. We employed the earlier developed CRAFT (Cre recombinase Reporter Assay For Translocation) assay to detect transfer of Cre::Vir fusion proteins from A. tumefaciens into plants, monitored by stable reconstitution of a kanamycin resistance marker, and into yeast, screened by loss of the URA3 gene. We show that the C-terminal 50 amino acids of VirE2 and VirE3 are sufficient to mediate Cre translocation into host cells, confirming earlier indications of a C-terminal transport signal. This transfer was independent of the presence or absence of VirE1. Besides, the translocation efficiency of VirF is not altered in a virE1 mutant. The results unambiguously show that the VirE1 chaperone is not essential for the recognition of the VirE2 transport signal by the transport system and the subsequent translocation across the bacterial envelope into host cells.
机译:根癌土壤杆菌使用IV型分泌系统将核蛋白复合物和效应蛋白直接传递到植物细胞中。单链DNA结合蛋白VirE2,F-box蛋白VirF和VirE3通过此VirB / D4编码的转运系统传递到宿主细胞中。 VirE1通过调节VirE2的有效翻译并防止VirE2-VirE2在细菌细胞中聚集来充当VirE2的伴侣。我们分析了VirE1分子伴侣是否对VirB / D4编码的IV型分泌系统对VirE2的转运识别也必不可少。此外,我们分析了是否也存在virE操纵子的VirF和VirE3易位受到不存在VirE1的影响。我们采用了较早开发的CRAFT(易位的Cre重组酶报告基因测定)试验来检测Cre :: Vir融合蛋白从根癌农杆菌向植物的转移,通过卡那霉素抗性标记物的稳定重组进行监测,并通过丧失URA3基因。我们显示,VirE2和VirE3的C端50个氨基酸足以介导Cre易位到宿主细胞中,证实了C端转运信号的早期迹象。此转移与VirE1的存在与否无关。此外,在virE1突变体中VirF的转运效率没有改变。结果清楚地表明,VirE1分子伴侣对于转运系统识别VirE2转运信号以及随后跨细菌包膜转运进入宿主细胞不是必需的。

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